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Shoc2tm1.2Mhan
Targeted Allele Detail
Summary
Symbol: Shoc2tm1.2Mhan
Name: Shoc2, leucine rich repeat scaffold protein; targeted mutation 1.2, Min Han
MGI ID: MGI:4459450
Synonyms: Sur-8delta
Gene: Shoc2  Location: Chr19:53932737-54021564 bp, + strand  Genetic Position: Chr19, 48.83 cM
Alliance: Shoc2tm1.2Mhan page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:161211
Parent Cell Line:  W4 (ES Cell)
Strain of Origin:  129S6/SvEvTac
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsHeterozygous Shoc2tm1.1Mhan animals were bred to PGK-cre transgenic mice to delete the loxP-flanked region, resulting in a null allele. (J:161211)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Shoc2 Mutation:  43 strains or lines available
References
Original:  J:161211 Yi J, et al., Endothelial SUR-8 acts in an ERK-independent pathway during atrioventricular cushion development. Dev Dyn. 2010 Jul;239(7):2005-13
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory